ENSMUSG00000026124


Mus musculus

Features
Gene ID: ENSMUSG00000026124
  
Biological name :Cfc1
  
Synonyms : Cfc1 / Cryptic protein / P97766
  
Possible biological names infered from orthology : CFC1B / cripto, FRL-1, cryptic family 1 / cripto, FRL-1, cryptic family 1B / P0CG36 / P0CG37
  
Species: Mus musculus
  
Chr. number: 1
Strand: 1
Band: B
Gene start: 34535648
Gene end: 34544313
  
Corresponding Affymetrix probe sets: 10345393 (MoGene1.0st)   1421524_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000027298
NCBI entrez gene - 12627     See in Manteia.
MGI - MGI:109448
RefSeq - NM_007685
RefSeq Peptide - NP_031711
swissprot - P97766
Ensembl - ENSMUSG00000026124
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 tdgf1ENSDARG00000035095Danio rerio
 CFC1ENSGALG00000012623Gallus gallus
 CFC1ENSG00000136698Homo sapiens
 CFC1BENSG00000152093Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Tdgf1 / teratocarcinoma-derived growth factor 1 / P13385*ENSMUSG0000003249426


Protein motifs (from Interpro)
Interpro ID Name
 IPR000742  EGF-like domain
 IPR013032  EGF-like, conserved site
 IPR019011  Cryptic/Cripto, CFC domain


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001889 liver development IMP
 biological_processGO:0001947 heart looping IMP
 biological_processGO:0003007 heart morphogenesis IMP
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0007368 determination of left/right symmetry IMP
 biological_processGO:0007369 gastrulation IEA
 biological_processGO:0007492 endoderm development IGI
 biological_processGO:0009791 post-embryonic development IMP
 biological_processGO:0009952 anterior/posterior pattern specification IGI
 biological_processGO:0030509 BMP signaling pathway IDA
 biological_processGO:0038092 nodal signaling pathway IMP
 biological_processGO:0048536 spleen development IMP
 biological_processGO:0048546 digestive tract morphogenesis IMP
 biological_processGO:0048856 anatomical structure development IGI
 biological_processGO:0060070 canonical Wnt signaling pathway IDA
 biological_processGO:0060413 atrial septum morphogenesis IMP
 biological_processGO:0060460 left lung morphogenesis IMP
 biological_processGO:0060541 respiratory system development IMP
 biological_processGO:0060976 coronary vasculature development IMP
 cellular_componentGO:0005576 extracellular region IEA
 cellular_componentGO:0005886 plasma membrane TAS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0031225 anchored component of membrane IEA
 molecular_functionGO:0038100 nodal binding ISO
 molecular_functionGO:0070697 activin receptor binding IPI


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000267 abnormal cardiac development "aberrant formation or incomplete differentiation of the heart" [MGI:cls, J:53370]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

 MP:0000284 double outlet right ventricle "both the aorta and the pulmonary trunk originate from the right ventricle, usually in conjunction with a ventricular septal defect" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:67826]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

Allelic Composition: Cfc1tm1Mms/Cfc1tm1Mms
Genetic Background: either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)

 MP:0000531 right pulmonary isomerism "bilaterally symmetric right lung pattern (or altered asymmetric patterning of the lung)" [ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator, J:58530]
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Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

Allelic Composition: Cfc1tm1Mms/Cfc1tm1Mms
Genetic Background: either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)

Allelic Composition: Cfc1b2b970Clo/Cfc1b2b970Clo
Genetic Background: C57BL/6J-Cfc1b2b970Clo

Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0000542 left-sided isomerism "the relative symmetry of the organs of the thorax and abdomen as indicated by both atria displaying the morphology of the left atrium" [ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator]
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Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0000598 abnormal liver morphology "malformation or absence of this bile-secreting exocrine gland, which is important for detoxification; for fat, carbohydrate, and protein metabolism; and for glycogen storage " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:23170]
Show

Allelic Composition: Bmp4tm1Jfm/Bmp4tm1.1Jfm,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129S4/SvJaeSor

 MP:0000644 dextrocardia "cardiac apex pointing to the right as opposed to the normal levocardia" [ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

Allelic Composition: Cfc1tm1Mms/Cfc1tm1Mms
Genetic Background: either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)

 MP:0000650 mesocardia "cardiac apex pointing to the middle as opposed to the normal levocardia" [ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator]
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Allelic Composition: Cfc1tm1Mms/Cfc1tm1Mms
Genetic Background: either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)

Allelic Composition: Cfc1b2b970Clo/Cfc1b2b970Clo
Genetic Background: C57BL/6J-Cfc1b2b970Clo

 MP:0000690 absent spleen "missing organ that functions to filter blood and to store red corpuscles and platelets" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:55583]
Show

Allelic Composition: Bmp4tm1Jfm/Bmp4tm1.1Jfm,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129S4/SvJaeSor

 MP:0000692 small spleen "decreased spleen size" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

 MP:0000694 spleen hypoplasia "small size due to reduced cell number in the spleen" [J:43971]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0001706 abnormal left-right axis patterning "anomaly in the formation or development of the body or a specific organ of the body in relation to the left and right sides of the body or organ" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Bmp4tm1Jfm/Bmp4tm1.1Jfm,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129S4/SvJaeSor

 MP:0002083 premature death "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Bmp4tm1Jfm/Bmp4tm1.1Jfm,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129S4/SvJaeSor

 MP:0002766 situs inversus "lateral transposition of the viscera of the thorax and abdomen, sometimes incomplete" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Cfc1tm1Mms/Cfc1tm1Mms
Genetic Background: either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)

 MP:0003342 accessory spleen "the splenic tissue is divided into equal masses; often related to situs inversus" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, ncbi:Matthew Mailman, NCBI request]
Show

Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0004110 transposition of great arteries "cardiovascular malformation in which the aorta arises from the right ventricle while the pulmonary artery arises from the left ventricle" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

Allelic Composition: Cfc1b2b970Clo/Cfc1b2b970Clo
Genetic Background: C57BL/6J-Cfc1b2b970Clo

 MP:0004113 abnormal aortic arch morphology "structural anomoly of the portion of the descending aorta proceeding from the arch of the aorta and extending to the diaphragm " [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0004133 heterotaxia "abnormal arrangement of organs or parts of the body in relation to each other" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
Show

Allelic Composition: Cfc1b2b970Clo/Cfc1b2b970Clo
Genetic Background: C57BL/6J-Cfc1b2b970Clo

Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0004158 right aortic arch "the aortic arch lies to the right of the trachea and esophagus; results from persistance of the entire right dorsal arch and involution of a segment of the left arch" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
Show

Allelic Composition: Cfc1tm1Mms/Cfc1tm1Mms
Genetic Background: either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)

 MP:0004190 abnormal direction of embryo turning "axial rotation of the embryo in a direction other than the normal anticlockwise direction when viewed towards the caudal pole during the late primitive streak/early somite stage (Mus E8.5-E9.5); clockwise rotation is frequently associated with heart and visceral defects" [ISBN:0-12-402035-6 "Kaufman, MH The Atlas of Mouse Development"]
Show

Allelic Composition: Cfc1tm1Mms/Cfc1tm1Mms
Genetic Background: either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)

 MP:0004252 abnormal direction of looping morphogenesis "deviation from the normal rightward direction of cardiac looping" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Cfc1tm1Mms/Cfc1tm1Mms
Genetic Background: either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)

 MP:0006063 abnormal inferior vena cava morphology "structural malformation in the principal vein draining blood from the lower portion of the body" [smb:Susan M Bello, Mouse Genome Informatics Curator, Taber s Cyclopedic Medical Dictionary:19th edition: ISBN N 0-8036-0655-99]
Show

Allelic Composition: Cfc1b2b970Clo/Cfc1b2b970Clo
Genetic Background: C57BL/6J-Cfc1b2b970Clo

 MP:0006113 abnormal heart septum morphology "abnormality in the wall between the atria or ventricles of the heart, usually incomplete closure" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

 MP:0010402 ventricular septal defect "abnormal communications between the two lower chambers of the heart, including such defects in the perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular regions" [MESH:C14.240.400.560.540]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0010403 atrial septal defect "abnormal communications between the two upper chambers of the heart, including such defects in any or all of the ostium primum, ostium secundum, sinus venosus, and coronary sinus regions" [MESH:C14.240.400.560.375]
Show

Allelic Composition: Cfc1tm1Mms/Cfc1tm1Mms
Genetic Background: either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)

 MP:0010406 absent atrial septum "absence of the thin membranous structure between the two heart atria" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0010412 atrioventricular septal defect "defects in the thin membranous structure between the right atrium and left ventricle that arise from faulty development of the embryonic endocardial cushions; the spectrum ranges from a primum atrial septal defect and cleft mitral valve, known as a partial atrioventricular septal defect (partial AVSD), to defects of both the primum atrial septum and inlet ventricular septum and the presence of a common atrioventricular valve, referred to as complete atrioventricular septal defect (complete AVSD)" [http://emedicine.medscape.com]
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Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0010413 complete atrioventricular septal defect "a type of atrioventricular septal defect in which a single atrioventricular valve annulus, a common atrioventricular valve, and a defect of the inlet ventricular septum are observed; deficiency of the atrioventricular septum also results in the presence of a large primum atrial septal defect" [http://emedicine.medscape.com]
Show

Allelic Composition: Cfc1b2b970Clo/Cfc1b2b970Clo
Genetic Background: C57BL/6J-Cfc1b2b970Clo

 MP:0010420 muscular ventricular septal defect "abnormal communications between the two lower chambers of the heart, involving the muscular septum and often occurring as multiple communications, and includes central muscular or midmuscular, apical, or marginal communications when the defect is along the RV-septal junction; any single defect observed from the LV aspect may have several openings on the RV aspect" [http://emedicine.medscape.com]
Show

Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0010422 heart right ventricle hypoplasia "underdevelopment or reduced size of the heart right ventricle, often due to a reduced number of cells" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0010426 abnormal heart and great artery attachment "any anomaly in the in the position or pattern of the connection site of the heart to any of the great arteries, including the pulmonary artery and aorta" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

 MP:0010443 total anomalous pulmonary venous connection, intracardiac "the pulmonary veins connect directly to the right side of heart (eg, coronary sinus or directly to the right atrium) instead of the left atrium" [http://emedicine.medscape.com]
Show

Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0010454 abnormal truncus arteriosis septation "anomaly in the process of dividing the common arterial trunk arising out of both heart ventricles to divide into the aorta and pulmonary artery during development" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

 MP:0010466 vascular ring "the trachea and esophagus are completely encircled by connected segments of the aortic arch and its branches" [http://emedicine.medscape.com]
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Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0010487 abnormal right subclavian artery morphology "any structural anomaly of the artery that normally extends from the brachiocephalic artery to the right side of the body" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0010808 right-sided stomach "stomach is present on the right side of the body instead of the left" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

Allelic Composition: Cfc1tm1Mms/Cfc1tm1Mms
Genetic Background: either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)

Allelic Composition: Cfc1b2b970Clo/Cfc1b2b970Clo
Genetic Background: C57BL/6J-Cfc1b2b970Clo

Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0011085 complete postnatal lethality "premature death anytime between the neonatal period and weaning age of all organisms of a given genotype in a population (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
Show

Allelic Composition: Prrxl1tm1And/Prrxl1tm1And
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J * CD-1

 MP:0011086 partial postnatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms anytime between the neonatal period and weaning age (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
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Allelic Composition: Cfc1tm1Mms/Cfc1tm1Mms
Genetic Background: either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)

 MP:0011254 superior-inferior ventricles "an abnormality in which the heart ventricles are in a superior-inferior relationship due to abnormal displacement of the ventricular mass along the horizontal plane of its long axis; this frequently occurs together with criss-cross atrio-ventricular relationships" [ISBN:0-683-40008-8, MGI:csmith]
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Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

 MP:0011569 abnormal azygos vein morphology "any structural anomaly of the unpaired vein which in humans arises from the right ascending lumbar vein or the vena cava, enters the thorax through the aortic orifice in the diaphragm, and terminates in the superior vena cava; unlike humans, mice have a single and left-sided azygos vein that develops from the paired embryonic cardinal venous system and drains most of the right and left thoracic walls into the left anterior vena cava" [MGI:anna]
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Allelic Composition: Cfc1tm1Mms/Cfc1tm1Mms
Genetic Background: either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)

 MP:0011665 d-loop transposition of the great arteries "complete transposition of the great arteries; the d- refers to the dextroposition of the bulboventricular loop (ie, the position of the right ventricle, which is on the right side); in addition, the aorta also tends to be on the right and anterior, and the great arteries are parallel rather than crossing" [PMID:17159076]
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Allelic Composition: Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo
Genetic Background: C57BL/6J-Cfc1b2b2736.1Clo

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000000532 Acvr1b / Q61271 / Activin receptor type-1B / P36896* / activin A receptor type 1B*  / complex
 ENSMUSG00000026124 Cfc1 / P97766 / Cryptic protein / CFC1B* / P0CG36* / P0CG37* / cripto, FRL-1, cryptic family 1* / cripto, FRL-1, cryptic family 1B*  / complex
 ENSMUSG00000026834 Acvr1c / Q8K348 / Activin receptor type-1C / Q8NER5* / activin A receptor type 1C*  / complex
 ENSMUSG00000038793 Q64280 / Lefty1 / Left-right determination factor 1 / LEFTY2* / O00292* / O75610* / left-right determination factor 2*  / complex / reaction
 ENSMUSG00000061393 Acvr2b / P27040 / Activin receptor type-2B / Q13705* / activin A receptor type 2B*  / complex
 ENSMUSG00000052155 Acvr2a / P27038 / Activin receptor type-2A / P27037* / activin A receptor type 2A*  / complex
 ENSMUSG00000037171 Nodal / P43021 / Q96S42* / nodal growth differentiation factor*  / complex / reaction
 ENSMUSG00000066652 P57785 / Lefty2 / Left-right determination factor 2 / LEFTY1* / O00292* / O75610* / left-right determination factor 1*  / complex / reaction
 ENSMUSG00000109523 Gdf1 / P20863 / Embryonic growth/differentiation factor 1 / CERS1* / P27544* / P27539* / ceramide synthase 1* / growth differentiation factor 1*  / complex / reaction






 

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